Canonical Allele Identifier: CA2626419897

Gene: VRK1

Linked Data

• gnomAD v4: 14-96875995-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.96875996_96875997insCT , CM000676.2:g.96875996_96875997insCT	GRCh38
NC_000014.8:g.97342333_97342334insCT , CM000676.1:g.97342333_97342334insCT	GRCh37
NC_000014.7:g.96412086_96412087insCT	NCBI36
NG_016293.1:g.83650_83651insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216639.8:c.1069-34_1069-33insCT MANE Select	ENSP00000216639.3:n.1069-34_1069-33insCT
ENST00000553683.2:c.1069-34_1069-33insCT	ENSP00000451412.2:n.1069-34_1069-33insCT
ENST00000555067.2:n.11089_11090insCT
ENST00000679365.1:c.1063-37_1063-36insCT	ENSP00000505882.1:n.1063-37_1063-36insCT
ENST00000679462.1:c.1070_1071insCT	ENSP00000506011.1:p.Ser358TyrfsTer7
ENST00000679506.1:n.3131-37_3131-36insCT
ENST00000679533.1:c.*842-34_*842-33insCT	ENSP00000505873.1:n.*842-34_*842-33insCT
ENST00000679650.1:c.*758-34_*758-33insCT	ENSP00000505156.1:n.*758-34_*758-33insCT
ENST00000679727.1:c.1063-34_1063-33insCT	ENSP00000505844.1:n.1063-34_1063-33insCT
ENST00000679758.1:c.1068+15261_1068+15262insCT	ENSP00000505539.1:n.1068+15261_1068+15262insCT
ENST00000679770.1:c.1069-34_1069-33insCT	ENSP00000505214.1:n.1069-34_1069-33insCT
ENST00000679816.1:c.1069-34_1069-33insCT	ENSP00000506525.1:n.1069-34_1069-33insCT
ENST00000679843.1:c.372-34_372-33insCT	ENSP00000506467.1:n.372-34_372-33insCT
ENST00000679903.1:c.1069-43_1069-42insCT	ENSP00000506022.1:n.1069-43_1069-42insCT
ENST00000679918.1:c.1069-34_1069-33insCT	ENSP00000505439.1:n.1069-34_1069-33insCT
ENST00000679941.1:c.1068+15261_1068+15262insCT	ENSP00000506520.1:n.1068+15261_1068+15262insCT
ENST00000679977.1:c.*315-34_*315-33insCT	ENSP00000504897.1:n.*315-34_*315-33insCT
ENST00000680007.1:c.1069-34_1069-33insCT	ENSP00000505683.1:n.1069-34_1069-33insCT
ENST00000680335.1:c.1068+15261_1068+15262insCT	ENSP00000505806.1:n.1068+15261_1068+15262insCT
ENST00000680387.1:c.1069-37_1069-36insCT	ENSP00000504908.1:n.1069-37_1069-36insCT
ENST00000680526.1:c.*587+15332_*587+15333insCT	ENSP00000505595.1:n.*587+15332_*587+15333insCT
ENST00000680538.1:c.979-34_979-33insCT	ENSP00000505611.1:n.979-34_979-33insCT
ENST00000680683.1:c.1069-34_1069-33insCT	ENSP00000506334.1:n.1069-34_1069-33insCT
ENST00000680724.1:c.1069-34_1069-33insCT	ENSP00000504891.1:n.1069-34_1069-33insCT
ENST00000680756.1:c.1069-34_1069-33insCT	ENSP00000506648.1:n.1069-34_1069-33insCT
ENST00000680849.1:c.1066-34_1066-33insCT	ENSP00000505602.1:n.1066-34_1066-33insCT
ENST00000680851.1:c.1069-5181_1069-5180insCT	ENSP00000505159.1:n.1069-5181_1069-5180insCT
ENST00000680922.1:c.*212+15261_*212+15262insCT	ENSP00000506480.1:n.*212+15261_*212+15262insCT
ENST00000680993.1:c.*432+15261_*432+15262insCT	ENSP00000505511.1:n.*432+15261_*432+15262insCT
ENST00000681061.1:c.692+15261_692+15262insCT
ENST00000681101.1:c.1069-34_1069-33insCT	ENSP00000506564.1:n.1069-34_1069-33insCT
ENST00000681195.1:c.1069-37_1069-36insCT	ENSP00000504933.1:n.1069-37_1069-36insCT
ENST00000681249.1:c.1069-37_1069-36insCT	ENSP00000506013.1:n.1069-37_1069-36insCT
ENST00000681344.1:c.1069-34_1069-33insCT	ENSP00000506151.1:n.1069-34_1069-33insCT
ENST00000681355.1:c.1069-34_1069-33insCT	ENSP00000506214.1:n.1069-34_1069-33insCT
ENST00000681363.1:c.*169-34_*169-33insCT	ENSP00000505564.1:n.*169-34_*169-33insCT
ENST00000681419.1:c.1069-34_1069-33insCT	ENSP00000505512.1:n.1069-34_1069-33insCT
ENST00000681474.1:c.890-34_890-33insCT	ENSP00000505569.1:n.890-34_890-33insCT
ENST00000681493.1:c.1063-34_1063-33insCT	ENSP00000506429.1:n.1063-34_1063-33insCT
ENST00000681524.1:c.*213-34_*213-33insCT	ENSP00000505783.1:n.*213-34_*213-33insCT
ENST00000681538.1:c.*238-34_*238-33insCT	ENSP00000506662.1:n.*238-34_*238-33insCT
ENST00000681598.1:c.*537+15261_*537+15262insCT	ENSP00000506128.1:n.*537+15261_*537+15262insCT
ENST00000681677.1:c.693-34_693-33insCT
ENST00000681695.1:c.*659-34_*659-33insCT	ENSP00000506225.1:n.*659-34_*659-33insCT
ENST00000681778.1:c.1068+15261_1068+15262insCT	ENSP00000506049.1:n.1068+15261_1068+15262insCT
ENST00000216639.7:c.1069-34_1069-33insCT	ENSP00000216639.3:n.1069-34_1069-33insCT
ENST00000555067.1:n.299-34_299-33insCT
ENST00000557222.5:c.637+15261_637+15262insCT
NM_003384.2:c.1069-34_1069-33insCT	NP_003375.1:n.1069-34_1069-33insCT
XM_006720247.2:c.1069-34_1069-33insCT	XP_006720310.1:n.1069-34_1069-33insCT
XM_011537132.1:c.1069-37_1069-36insCT	XP_011535434.1:n.1069-37_1069-36insCT
XM_006720247.4:c.1069-34_1069-33insCT	XP_006720310.1:n.1069-34_1069-33insCT
XM_017021624.2:c.1069-37_1069-36insCT	XP_016877113.1:n.1069-37_1069-36insCT
XM_017021625.1:c.1075-34_1075-33insCT	XP_016877114.1:n.1075-34_1075-33insCT
XR_001750539.2:n.1016-34_1016-33insCT
NM_003384.3:c.1069-34_1069-33insCT MANE Select	NP_003375.1:n.1069-34_1069-33insCT